A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18207395



Internal ID20774436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:170135203..170148654hg38UCSC Ensembl
chr2:170991713..171005164hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg3813452
hg1913452
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6337059
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18207395
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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